Convatec logo
Convatec

Pioneering trusted medical solutions to improve the lives we touch

Clinical Strategy Lead

StrategyStrategyFull TimeRemoteSeniorTeam 5,001-10,000Since 1978H1B SponsorCompany SiteLinkedIn

Location

District Of Columbia + 3 moreAll locations: District Of Columbia | Illinois | New York | Massachusetts

Posted

15 hours ago

Salary

$124.8K - $195K / year

Seniority

Senior

Bachelor Degree3 yrs expEnglish

Job Description

Clinical Strategy Lead

Convatec

• Act as a clinical strategist for our Advanced Wound Care Medical and Clinical Affairs team, with a special focus on emerging Advanced Wound Care technologies • Play a lead role in clinical study design, including regulatory approvals, statistical analysis plan, and budget • Close collaboration with Global Medical Education and Key Opinion Leader Management colleagues and Business Development and Marketing teams through interactions with key opinion leaders, healthcare providers, and regulatory bodies to analyze and identify unmet needs in our field • Work closely with the clinical operations colleagues to translate business strategies to actionable clinical study protocols and retrospective data generation plans • Analyze data output from clinical studies and other evidence generation activities and distill these into a cohesive "story" to be presented when needed • Play a proactive role in putting together publications and evidence communication in close collaboration with the medical writing team • Act as an educator and role model for colleagues outside of medical affairs • Support all our general medical affairs activities, including, but not limited to new product development, evidence generation and review, risk management, and other activities as needed • Act as a subject matter expert in the product line

Job Requirements

  • Bachelor’s degree or higher degree in Medicine, Life Sciences, Allied Health, Pharmacy, or Nursing
  • Advanced degree (MD, PhD MSN, DNP) preferred
  • Clinical experience or specialty knowledge in wound care preferred
  • At least 3 years’ experience in the medical device or pharmaceutical industry in positions of increasing responsibility
  • Strong understanding of clinical research, including literature reviews, protocol development, general study execution, and statistical analysis
  • Experience in clinical study design in an industry or academic setting
  • Understanding of the medical device industry: product development, pre-clinical, clinical, quality, marketing, and regulatory components
  • Experience with regulatory requirements for clinical studies in the US and EU is highly desirable
  • Strong computer skills and high level of proficiency of Microsoft Office
  • Ability to communicate fluently in English

Benefits

  • health benefits for individuals, families, and domestic partners, including medical, prescription drug, dental, and vision coverage
  • paid vacation
  • holidays
  • community service days
  • sick time
  • paid caregiver/parental leave
  • medical leave
  • retirement savings plan with company match

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